Canonical Allele Identifier: CA418279799
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68904672G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438989G>T , CM000663.2:g.68438989G>T GRCh38
NC_000001.10:g.68904672G>T , CM000663.1:g.68904672G>T GRCh37
NC_000001.9:g.68677260G>T NCBI36
NG_008472.1:g.15971C>A
NG_008472.2:g.15971C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.951C>A MANE Select ENSP00000262340.5:p.Thr317=
ENST00000262340.5:c.951C>A ENSP00000262340.5:p.Thr317=
NM_000329.2:c.951C>A NP_000320.1:p.Thr317=
XM_017002027.1:c.675C>A XP_016857516.1:p.Thr225=
NM_000329.3:c.951C>A MANE Select NP_000320.1:p.Thr317=